Taiwan FDA registration 018b2f560afa4cbca5a7405a75c7ea4f
“CareFusion” V. Mueller Nonpowered neurosurgical instrument (Non-Sterile)
TW: “客愛福生”密米樂非動力式神經外科用器械 (未滅菌)
Taiwan·Risk Class 1·MD·CareFusion·Registered Mar 11, 2019 – Mar 11, 2024ExpiredRegistration details
- Analysis ID
- 018b2f560afa4cbca5a7405a75c7ea4f
- License Form
- Ministry of Health Medical Device Import No. 020166
- Customs Code
- DHA09402016606
Company information
- Manufacturer
- CareFusion
- Manufacturer Country
- United States
- Authorized Representative
- BESPRING INTERNATIONAL MARKETING CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K4535 Non-powered neurosurgical instruments
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 11, 2019
- Expiry Date
- Mar 11, 2024
About this record
Access comprehensive regulatory information for “CareFusion” V. Mueller Nonpowered neurosurgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 018b2f560afa4cbca5a7405a75c7ea4f and manufactured by CareFusion. The authorized representative in Taiwan is BESPRING INTERNATIONAL MARKETING CO., LTD..
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